| Are you an individual who is inspired by new challenges, thrives in a fast-paced environment, and is seeking a career at the forefront of medical innovation? If this describes you, we encourage you to apply for the position of Veterinary Pathologist at American Preclinical Services (APS). Located in a northern suburb of Minneapolis, MN, APS is a dynamic, growing company specializing in medical device and pharmaceutical testing. APS is a full service, AAALAC and ISO 17025 accredited, USDA registered and GLP-compliant Contract Research Organization (CRO). The successful candidate will join a team of five anatomic pathologists at APS. Responsibilities: Performs duties related to pathology services in a preclinical, GLP research setting with regard to safety, biocompatibility and systemic toxicity studies conducted in compliance with applicable FDA and other national and international regulatory agency standards. This includes: - Interpreting gross, microscopic, and clinical pathology study data
- Consulting with clients and study directors on pathology findings
- Completing timely and accurate protocol-driven pathology reports
- Developing pathology methodologies, study designs and animal models for protocols
- Collaborating with facility veterinarians to generate diagnostic pathology data and interpretation of results in support of colony health objectives and needs
- Performing necropsy and gross dissections in conjunction with necropsy personnel, as needed
Qualifications: - Doctor of Veterinary Medicine (DVM/VMD) or Doctor of Medicine (MD) from an accredited university is required.
- Board certification in anatomic pathology by the American College of Veterinary Pathologists (ACVP), the European College of Veterinary Pathologists (ECVP), or equivalent bodies is desired.
- Two or more years of implantable medical device pathology or toxicological pathology experience with a broad knowledge of animal models (goats, cattle, swine, sheep, rabbits, rodents and dogs) or experience in medical device design/utilization or pharmaceutical development/utilization within a related industry is desirable.
- In-depth knowledge of GLP regulations and FDA medical device preclinical guidance documents is highly desirable.
- Excellent oral and written communication skills. Demonstrated statistical, analytical, project management, and scientific writing skills as evidenced by scientific publications and/or successful medical device or pharmaceutical regulatory submissions is preferred.
- Working knowledge of word processing, spreadsheet, and digital imaging/morphometry software.
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